01
Initial screening
We identify your training level, institution, research stage, deadline, and applicable rules—without collecting sensitive research data too early.
How it works
A visible process. Clear roles. No hidden handoff.
ProWrite separates screening, technical work, review, and approval so your project remains scientifically and institutionally defensible.
02
Research diagnostic
We assess objectives, methodology, documents, data, statistics, manuscript status, and the exact support your project needs.
03
Scope agreement
You receive clear deliverables, exclusions, responsibilities, timelines, revision limits, privacy terms, and disclosure requirements.
04
Project plan
We set checkpoints, document requirements, reviewer roles, a data-security plan, and—when needed—a statistical analysis plan.
05
Supervised development
Technical work proceeds in stages. You provide verified inputs, make scientific decisions, and review material outputs.
06
Independent quality checks
Applicable medical, methodological, statistical, editorial, reference, privacy, and cross-document checks are completed.
07
Researcher teach-back
Before release, you should be able to explain the problem, design, variables, analyses, findings, limitations, and conclusions.
08
Finalization & follow-up
You approve final files, contribution and disclosure language, retention actions, and the scope of post-delivery support.
Final-release review
First drafts are never automatic deliverables.
The final review mix depends on scope, but every material output has a documented human approval gate.
Scientific review
Clinical coherence and accurate claims
Methodological review
Objectives, design, variables, and methods align
Statistical review
Analyses, assumptions, denominators, and interpretation
Editorial review
Structure, clarity, terminology, and reporting
Evidence review
Citations support the adjacent claim
Privacy review
Minimum necessary data and no unsafe identifiers
Client teach-back
Your ability to explain the work is part of quality.
Before final delivery, you should be able to explain the research problem, objectives, study design, population, variables, statistical methods, findings, limitations, conclusions, and clinical implications.
Assess your current stage